Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/170272
Title: Active plane modulation of Bi₂O₃ nanosheets via Zn substitution for efficient electrocatalytic CO₂ reduction to formic acid
Authors: Liu, Yumei
Wu, Tiantian
Cheng, Hongfei
Wu, Jiawen
Guo, Xiaodong
Fan, Hong Jin
Keywords: Science::Chemistry
Issue Date: 2023
Source: Liu, Y., Wu, T., Cheng, H., Wu, J., Guo, X. & Fan, H. J. (2023). Active plane modulation of Bi₂O₃ nanosheets via Zn substitution for efficient electrocatalytic CO₂ reduction to formic acid. Nano Research, 16(8), 10803-10809. https://dx.doi.org/10.1007/s12274-023-5824-6
Project: RG 85/20 
RG 125/21
Journal: Nano Research
Abstract: Formic acid is considered one of the most economically viable products for electrocatalytic CO2 reduction reaction (CO2RR). However, developing highly active and selective electrocatalysts for effective CO2 conversion remains a grand challenge. Herein, we report that structural modulation of the bismuth oxide nanosheet via Zn2+ cooperation has a profound positive effect on exposure of the active plane, thereby contributing to high electrocatalytic CO2RR performance. The obtained Zn-Bi2O3 catalyst demonstrates superior selectivity towards formate generation in a wide potential range; a high Faradaic efficiency of 95% and a desirable partial current density of around 20 mA·cm−2 are obtained at −0.9 V (vs. reversible hydrogen electrode (RHE)). As proposed by density functional theory calculations, Zn substitution is the most energetically feasible for forming and stabilizing the key OCHO* intermediate among the used metal ions. Moreover, the more negative adsorption energy of OCHO* and the relatively low energy barrier for the desorption of HCOOH* are responsible for the enhanced activity and selectivity.
URI: https://hdl.handle.net/10356/170272
ISSN: 1998-0124
DOI: 10.1007/s12274-023-5824-6
Schools: School of Physical and Mathematical Sciences 
Rights: © 2023 Tsinghua University Press. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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